Treffer 1 - 20 von 31 für Suche 'LAUNER MARGARET', Suchdauer: 3,03s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3

    Inherited causes of clonal haematopoiesis in 97,691 whole genomes von Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

    Veröffentlicht in Nature (London)

    Volltext
    Artikel
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8

    Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities von Armstrong, Nicola J., Mather, Karen A., Sargurupremraj, Muralidharan, Knol, Maria J., Malik, Rainer, Satizabal, Claudia L., Yanek, Lisa R., Wen, Wei, Gudnason, Vilmundur G., Dueker, Nicole D., Elliott, Lloyd T., Hofer, Edith, Bis, Joshua, Jahanshad, Neda, Li, Shuo, Logue, Mark A., Luciano, Michelle, Scholz, Markus, Smith, Albert V., Trompet, Stella, Vojinovic, Dina, Xia, Rui, Alfaro-Almagro, Fidel, Ames, David, Amin, Najaf, Amouyel, Philippe, Beiser, Alexa S., Brodaty, Henry, Deary, Ian J., Fennema-Notestine, Christine, Gampawar, Piyush G., Gottesman, Rebecca, Griffanti, Ludovica, Jack, Clifford R., Jenkinson, Mark, Jiang, Jiyang, Kral, Brian G., Kwok, John B., Lampe, Leonie, C.M. Liewald, David, Maillard, Pauline, Marchini, Jonathan, Bastin, Mark E., Mazoyer, Bernard, Pirpamer, Lukas, Rafael Romero, José, Roshchupkin, Gennady V., Schofield, Peter R., Schroeter, Matthias L., Stott, David J., Thalamuthu, Anbupalam, Trollor, Julian, Tzourio, Christophe, van der Grond, Jeroen, Vernooij, Meike W., Witte, Veronica A., Wright, Margaret J., Yang, Qiong, Morris, Zoe, Siggurdsson, Siggi, Psaty, Bruce, Villringer, Arno, Schmidt, Helena, Haberg, Asta K., van Duijn, Cornelia M., Jukema, J. Wouter, Dichgans, Martin, Sacco, Ralph L., Wright, Clinton B., Kremen, William S., Becker, Lewis C., Thompson, Paul M., Mosley, Thomas H., Wardlaw, Joanna M., Ikram, M. Arfan, Adams, Hieab H.H., Seshadri, Sudha, Sachdev, Perminder S., Smith, Stephen M., Launer, Lenore, Longstreth, William, DeCarli, Charles, Schmidt, Reinhold, Fornage, Myriam, Debette, Stephanie, Nyquist, Paul A.

    Veröffentlicht in Stroke (1970)

    Volltext
    Artikel
  9. 9

    Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function von Wyss, Annah B., Sofer, Tamar, Lee, Mi Kyeong, Terzikhan, Natalie, Nguyen, Jennifer N., Lahousse, Lies, Latourelle, Jeanne C., Smith, Albert Vernon, Bartz, Traci M., Gao, Wei, Ahluwalia, Tarunveer S., Tang, Wenbo, Oldmeadow, Christopher, Duan, Qing, de Jong, Kim, Wojczynski, Mary K., Wang, Xin-Qun, Noordam, Raymond, Hartwig, Fernando Pires, Jackson, Victoria E., Wang, Tianyuan, Obeidat, Ma’en, Hobbs, Brian D., Huan, Tianxiao, Gui, Hongsheng, Parker, Margaret M., Hu, Donglei, Mogil, Lauren S., Kichaev, Gleb, Jin, Jianping, Graff, Mariaelisa, Harris, Tamara B., Kalhan, Ravi, Heckbert, Susan R., Paternoster, Lavinia, Burkart, Kristin M., Liu, Yongmei, Holliday, Elizabeth G., Wilson, James G., Vonk, Judith M., Barr, R. Graham, de Mutsert, Renée, Menezes, Ana Maria Baptista, Adams, Hieab H. H., van den Berge, Maarten, Joehanes, Roby, Levin, Albert M., Liberto, Jennifer, Launer, Lenore J., Morrison, Alanna C., Sitlani, Colleen M., Celedón, Juan C., Kritchevsky, Stephen B., Scott, Rodney J., Christensen, Kaare, Rotter, Jerome I., Bonten, Tobias N., Wehrmeister, Fernando César, Bossé, Yohan, Xiao, Shujie, Oh, Sam, Franceschini, Nora, Brody, Jennifer A., Kaplan, Robert C., Lohman, Kurt, McEvoy, Mark, Province, Michael A., Rosendaal, Frits R., Taylor, Kent D., Nickle, David C., Williams, L. Keoki, Burchard, Esteban G., Wheeler, Heather E., Sin, Don D., Gudnason, Vilmundur, North, Kari E., Fornage, Myriam, Psaty, Bruce M., Myers, Richard H., O’Connor, George, Hansen, Torben, Laurie, Cathy C., Cassano, Patricia A., Sung, Joohon, Kim, Woo Jin, Attia, John R., Lange, Leslie, Boezen, H. Marike, Thyagarajan, Bharat, Rich, Stephen S., Mook-Kanamori, Dennis O., Horta, Bernardo Lessa, Uitterlinden, André G., Im, Hae Kyung, Cho, Michael H., Brusselle, Guy G., Gharib, Sina A., Dupuis, Josée, Manichaikul, Ani, London, Stephanie J.

    Veröffentlicht in Nature communications

    Volltext
    Artikel
  10. 10

    Common variants at 12q14 and 12q24 are associated with hippocampal volume von Bis, Joshua C, DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M, Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F J, DeStefano, Anita L, Lambert, Jean-Charles, Jack, Jr, Clifford R, Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A, Fleischman, Debra, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H, Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark A, de Bruijn, Renée F A G, Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J, Chibnik, Lori B, Gislason, Gauti K, Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B, Phan, Thanh G, Oostra, Ben A, Stein, Jason L, Medland, Sarah E, Vasquez, Alejandro Arias, Hibar, Derrek P, Wright, Margaret J, Franke, Barbara, Martin, Nicholas G, Thompson, Paul M, Nalls, Michael A, Uitterlinden, Andre G, Au, Rhoda, Elbaz, Alexis, Beare, Richard J, van Swieten, John C, Lopez, Oscar L, Harris, Tamara B, Chouraki, Vincent, Breteler, Monique M B, De Jager, Philip L, Becker, James T, Vernooij, Meike W, Knopman, David, Fazekas, Franz, Wolf, Philip A, van der Lugt, Aad, Gudnason, Vilmundur, Longstreth, Jr, W T, Brown, Matthew A, Bennett, David A, van Duijn, Cornelia M, Mosley, Thomas H, Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J, Ikram, M Arfan, Seshadri, Sudha

    Veröffentlicht in Nature genetics

    Volltext
    Artikel
  11. 11
  12. 12
  13. 13
  14. 14

    A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease von Zhang, Xiaoling, Ma, Yiyi, Lancour, Daniel, Farrell, John J., Chung, Jaeyoon, Dinh, Huyen, Doddapeneni, Harsha, English, Adam, Gibbs, Richard A., Han, Yi, Jayaseelan, Joy, Kalra, Divya, Khan, Ziad, Lee, Sandra, Liu, Yue, Muzny, Donna, Nasser, Waleed, White, Simon, Worley, Kim, Zhu, Yiming, Beiser, Alexa, Chen, Yuning, Chung, Jaeyoon, Cupples, L. Adrienne, DeStefano, Anita, Dupuis, Josee, Farrell, John, Farrer, Lindsay, Lancour, Daniel, Lin, Honghuang, Sarnowski, Chloe, Zhang, Xiaoling, Choi, Seung Hoan, Gabriel, Stacey, Butkiewicz, Mariusz, Haines, Jonathan, Song, Yeunjoo, Barral, Sandra, Reitz, Christiane, Reyes, Dolly, Tosto, Giuseppe, Vardarajan, Badri, Amad, Shahzad, Amin, Najaf, Ikram, M. Afran, van Duijn, Cornelia, Vanderspek, Ashley, Schmidt, Helena, Goate, Alison, Marcora, Edoardo, Foroud, Tatiana, Feolo, Michael, Launer, Lenore J., Bennett, David A., Xia, Li Charlie, Beecham, Gary, Hamilton-Nelson, Kara, Jaworski, James, Martin, Eden, Pericak-Vance, Margaret, Rajabli, Farid, Schmidt, Michael, Cantwell, Laura, Childress, Micah, Chou, Yi-Fan, Cweibel, Rebecca, Leung, Yuk Yee, Lin, Han-Jen, Malamon, John, Naj, Adam, Valladares, Otto, Wang, Li-San, Wang, Weixin, Zhang, Nancy, Boerwinkle, Eric, Bressler, Jan, Fornage, Myriam, Jian, Xueqiu, Liu, Xiaoming, Blue, Elizabeth, Brown, Lisa, Day, Tyler, Dorschner, Michael, Horimoto, Andrea R., Nato, Alejandro Q., Navas, Pat, Nguyen, Hiep, Rice, Kenneth, Sohi, Harkirat, Thornton, Timothy, Tsuang, Debby, Cruchaga, Carlos, Fulton, Robert S., Koboldt, Daniel C., Larson, David E., Waligorski, Jason, Wilson, Richard K., Haines, Jonathan L., Pericak-Vance, Margaret A., Lunetta, Kathryn L.

    Veröffentlicht in Alzheimer's & dementia

    Volltext
    Artikel
  15. 15
  16. 16

    A genome‐wide association meta‐analysis of all‐cause and vascular dementia von Damotte, Vincent, Skrobot, Olivia, Bis, Joshua C., Li, Gloria Hoi‐Yee, Yang, Jingyun, Alessandra, Bizzarro, Chai, Yuek Ling, Knol, M. J., Concas, Maria Pina, Giorgia, Girotto, Riaz, Moeen, Naj, Adam C, Gireud‐Goss, Monica, Wadop, Yannick N., Gudnason, Vilmundur, Battista, Petronilla, Santin, Aurora, Sardone, Rodolfo, Launer, Lenore, Bressler, Jan, Grand, Quentin Le, Caro, Ilana, Roshchupkin, Gennady V., Yang, Chaojie, Bartz, Traci M., Nalls, Mike A., Rich, Stephen S., Setten, Jessica, Vugt, Marion, Grabe, Hans J., Jukema, J Wouter, Wassertheil‐Smoller, Sylvia, Longstreth, W T., Sattar, Naveed, Romero, Jose R, Lioutas, Vasileios, Wang, Ruiqi, Marquié, Marta, Pytel, Vanesa Veronica, Tàrraga, Lluís, Garcia‐Ribas, Guillermo, Pérez‐Tur, Jordi, Real, Luis Miguel, Sáez, María Eugenia, Bullido, María J., Álvarez, Victoria, Küçükali, Fahri, Düzel, Emrah, Wagner, Michael, Grimmer, Timo, Moreno, Fermin, Real, Luis M, Mendonça, Alexandre, Hort, Jakub, Papenberg, Goran, Nordestgaard, Børge G., Kivipelto, Miia, Haapasalo, Annakaisa, Nicolas, Gael, Grünblatt, Edna, Galimberti, Daniela, Mecocci, Patrizia, Tremolizzo, Lucio, Seripa, Davide, Engelborghs, Sebastiaan, Vandenberghe, Rik, Ingelsson, Martin, Lai, Mitchell K. P., Tan, Boon‐Yeow, Cefalù, Angelo Baldassare, Armstrong, Nicola J, Bordet, Anne‐Marie, Brodaty, Henry, D'Onofrio, Grazia, Esiri, Margaret, Gelé, Patrick, Masullo, Carlo, Mather, Karen A, Monastero, Roberto, Panza, Francesco, Sachdev, Perminder S, Thalamuthu, Anbupalam, Tybjærg‐Hansen, Anne, Thomas, Laurent F, Pedersen, Linda M, Bosnes, Ingunn, Duijn, Cornelia, Chen, Christopher, Kamboh, M. Ilyas, Satizabal, Claudia, Adams, Hieab, Hveem, Kristian, Dufouil, Carole, Zwart, John‐Anker, Fornage, Myriam, Winsvold, Bendik, Ruiz, Agustin, Kehoe, Patrick G., Weinstein, Galit, Seshadri, Sudha

    Veröffentlicht in Alzheimer's & dementia

    Volltext
    Artikel
  17. 17

    Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume von Vojinovic, Dina, Adams, Hieab H., Jian, Xueqiu, Yang, Qiong, Smith, Albert Vernon, Bis, Joshua C., Teumer, Alexander, Scholz, Markus, Armstrong, Nicola J., Hofer, Edith, Saba, Yasaman, Luciano, Michelle, Bernard, Manon, Trompet, Stella, Yang, Jingyun, Gillespie, Nathan A., van der Lee, Sven J., Neumann, Alexander, Ahmad, Shahzad, Andreassen, Ole A., Ames, David, Amin, Najaf, Arfanakis, Konstantinos, Bastin, Mark E., Becker, Diane M., Beiser, Alexa S., Beyer, Frauke, Brodaty, Henry, Bryan, R. Nick, Bülow, Robin, Dale, Anders M., De Jager, Philip L., Deary, Ian J., DeCarli, Charles, Fleischman, Debra A., Gottesman, Rebecca F., van der Grond, Jeroen, Gudnason, Vilmundur, Harris, Tamara B., Homuth, Georg, Knopman, David S., Kwok, John B., Lewis, Cora E., Li, Shuo, Loeffler, Markus, Lopez, Oscar L., Maillard, Pauline, El Marroun, Hanan, Mather, Karen A., Mosley, Thomas H., Muetzel, Ryan L., Nauck, Matthias, Nyquist, Paul A., Panizzon, Matthew S., Pausova, Zdenka, Psaty, Bruce M., Rice, Ken, Rotter, Jerome I., Royle, Natalie, Satizabal, Claudia L., Schmidt, Reinhold, Schofield, Peter R., Schreiner, Pamela J., Sidney, Stephen, Stott, David J., Thalamuthu, Anbupalam, Uitterlinden, Andre G., Valdés Hernández, Maria C., Vernooij, Meike W., Wen, Wei, White, Tonya, Witte, A. Veronica, Wittfeld, Katharina, Wright, Margaret J., Yanek, Lisa R., Tiemeier, Henning, Kremen, William S., Bennett, David A., Jukema, J. Wouter, Paus, Tomas, Wardlaw, Joanna M., Schmidt, Helena, Sachdev, Perminder S., Villringer, Arno, Grabe, Hans Jörgen, Longstreth, W T, van Duijn, Cornelia M., Launer, Lenore J., Seshadri, Sudha, Ikram, M Arfan, Fornage, Myriam

    Veröffentlicht in Nature communications

    Volltext
    Artikel
  18. 18
  19. 19

    Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities von Armstrong, Nicola J, Mather, Karen A, Sargurupremraj, Muralidharan, Knol, Maria J, Malik, Rainer, Satizabal, Claudia L, Yanek, Lisa R, Wen, Wei, Gudnason, Vilmundur G, Dueker, Nicole D, Elliott, Lloyd T, Hofer, Edith, Bis, Joshua, Jahanshad, Neda, Li, Shuo, Logue, Mark A, Luciano, Michelle, Scholz, Markus, Smith, Albert V, Trompet, Stella S, Vojinovic, Dina, Xia, Rui, Alfaro-Almagro, Fidel, Ames, David, Amin, Najaf, Amouyel, Philippe, Beiser, Alexa S, Brodaty, Henry, Deary, Ian J, Fennema-Notestine, Christine, Gampawar, Piyush G, Gottesman, Rebecca, Griffanti, Ludovica, Jnr, Clifford R Jack, Jenkinson, Mark, Jiang, Jiyang, Kral, Brian G, Kwok, John B, Lampe, Leonie, Liewald, David CM, Maillard, Pauline, Marchini, Jonathan, Bastin, Mark E, Mazoyer, Bernard, Pirpamer, Lukas, Romero, José Rafael, Roshchupkin, Gennady V, Schofield, Peter R, Schroeter, Matthias L, Stott, David J, Thalamuthu, Anbupalam, Trollor, Julian, Tzourio, Christophe, van der Grond, Jeroen, Vernooij, Meike W, Witte, Veronica A, Wright, Margaret J, Yang, Qiong, Morris, Zoe, Siggurdsson, Siggi, Psaty, Bruce, Villringer, Arno, Schmidt, Helena, Haberg, Asta K, van Duijn, Cornelia M, Jukema, J Wouter, Dichgans, Martin, Sacco, Ralph L, Wright, Clinton B, Kremen, William S, Becker, Lewis C, Thompson, Paul M, Mosley, Thomas H, Wardlaw, Joanna M, Ikram, M Arfan, Adams, Hieab HH, Seshadri, Sudha, Sachdev, Perminder S, Smith, Stephen M, Launer, Lenore, Longstreth, William, DeCarli, Charles, Schmidt, Reinhold, Fornage, Myriam, Debette, Stephanie, Nyquist, Paul A

    Veröffentlicht in Stroke (1970)

    Volltext
    Artikel
  20. 20

    Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed von Keener, Rebecca, Iyer, Kruthika R., Weinstock, Joshua S., Lane, John, Miller-Fleming, Tyne W., Brody, Jennifer A., Raffield, Laura M., McHugh, Caitlin P., Jain, Deepti, Gogarten, Stephanie M., Laurie, Cecelia A., Keramati, Ali, Arvanitis, Marios, Smith, Albert V., Heavner, Benjamin, Bis, Joshua C., Blangero, John, Burchard, Esteban G., Celedón, Juan C., Chang, Yen Pei C., de las Fuentes, Lisa, DeMeo, Dawn L., Garrett, Melanie E., Hidalgo, Bertha A., Irvin, Marguerite R., Islam, Talat, Johnson, W. Craig, Kaab, Stefan, Launer, Lenore, Liu, Simin, Moscati, Arden, North, Kari E., Rafaels, Nicholas, Seidman, Christine, Weeks, Daniel E., Wen, Fayun, Wheeler, Marsha M., Williams, L. Keoki, Zhao, Wei, Aslibekyan, Stella, Auer, Paul L., Bowden, Donald W., Cade, Brian E., Cho, Michael H., Curran, Joanne E., Daya, Michelle, Deka, Ranjan, Eng, Celeste, Fingerlin, Tasha E., Guo, Xiuqing, Hou, Lifang, Johnsen, Jill M., Kenny, Eimear E., Liu, Chunyu, Minster, Ryan L., Nouraie, Mehdi, Smith, Jennifer A., Smith, Nicholas L., Lasky-Su, Jessica, Taylor, James G., Telen, Marilyn J., White, Marquitta J., Zhang, Yingze, Wiggins, Kerri L., Weiss, Scott T., Vasan, Ramachandran S., Taylor, Kent D., Sinner, Moritz F., Sheu, Wayne H.-H., Schwartz, David A., Raby, Benjamin A., Palmer, Nicholette D., Nekhai, Sergei, Montgomery, Courtney G., Mitchell, Braxton D., Meyers, Deborah A., Kumar, Rajesh, Konkle, Barbara A., Kelly, Shannon, Kaplan, Robert, He, Jiang, Gelb, Bruce D., Fornage, Myriam, Correa, Adolfo, Boerwinkle, Eric, Ashley-Koch, Allison E., Arnett, Donna K., Albert, Christine, Laurie, Cathy C., Abecasis, Goncalo, Nickerson, Deborah A., Wilson, James G., Levy, Daniel, Ruczinski, Ingo, Aviv, Abraham, Thornton, Timothy, O’Connell, Jeff, Armanios, Mary, Pankratz, Nathan, Mathias, Rasika A.

    Veröffentlicht in Cell genomics

    Volltext
    Artikel